Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
  • C07D498/18—Bridged systems

Definitions

• the compounds of the invention show a high degree of antibacterial activity in vitro, as it is apparent from table I, in lo which the minimal inhibitory concentration in p.g./m
• mice with experimental infection induced by Staphylococcus aureus, have been 15 recorded in table I.
• the substances can be ad ministered both by systemic and topical route, although this latter route may be preferred, as said above, because of the 20 light color.
• infectious diseases such as pneumonia, abscess, phlegmon, furuncles,
• reaction is carried out in an organic inert solvent at room temperature for a period oftime of7 to 20 hours.
• the new rifamycins are generally well crystallized substances and show a better stability in the time than the other rifamycins and are much lighter in color than the parent compounds, being straw to amber yellow. As a rule they do not have a well defined melting point and decompose above I50 otite, osteomyelitis, cystitis, cholecystitis, liver infections and so on.
• compositions may contain unit doses of 50 to 500 mg. of the substances.
• the substances may be filled into capsules or incorporated in tablets and suppositories; or alternatively they may be suspended to form syrups or suspensions to be employed as drops.
• aqueous suspensions or ointments may be applied, in which the concentration of the active ingredient may vary within broad limits, e.g. between 0.5 and 10 percent.
• the solution is concentrated to one-fourth of its volume.
• the liquid is poured, while stirring, into 350 ml. of a 2 percent aqueous solution of ascorbic acid, so as to convert rifamycin S, which might be still present, into the corresponding reduced form i.e., the rifamycin SV.
• the pH is adjusted to 2-3 and the rifamycins are extracted with 400 ml. of ethyl acetate.
• the organic phase is rendered anhydrous with the aid of powdered sodium sulfate, concentrated to dryness in vacuo, .and the residue is taken up in ml. of chloroform.
• the solution is chromatographed on a column of silica-gel and eluted with a mixture of chlorofonn-ethanol 9:1.
• the first 100 ml. colored fraction is discarded, while the next three fractions of 100 ml. each, are combined and evaporated to dryness.
• the residue is dissolved in 3035 ml. of methanol. From this solution cooled at 0-5 C. for 2-3 hours, the final compound precipitates, as light amber colored crystals, which are collected, washed with methanol and dried in vacuo at 40-45 C. 7
• EXAMPLE 18 A suppository is prepared by incorporating 200 mg. of l,2'-
• a dermatologic ointment is prepared from:
• R is selected from the class consisting of hydrogen, lower alkyl of one to three carbon atoms, hydroxyethyl, phenyl and benzyl, R is lower alkyl with one to three carbon atoms, and R" is selected from the class consisting of methyl,
• rifamycin SV derivative is l',2-dimethyl-3'-carbomethoxypyrrole-[ 3,2c 1-4 -deoxyrifamycin.
• rifamycin SV derivative is l',2-dimethyl-3'-dimethylcarbamylpyrrole-[ 3,2- c1-4-deoxyrifamycin.
• rifamycin SV derivative is l,2'-dimethyl-3-carbeth

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Medicinal Preparation (AREA)

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Publications (1)

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ID=9878162

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Citations (1)

• 1967
  • 1967-03-01 GB GB9755/67A patent/GB1172155A/en not_active Expired
• 1968
  • 1968-02-05 US US702796A patent/US3625961A/en not_active Expired - Lifetime
  • 1968-02-08 IL IL29441A patent/IL29441A/en unknown
  • 1968-02-17 DE DE19681695384 patent/DE1695384A1/de not_active Withdrawn
  • 1968-02-20 NL NL6802429A patent/NL6802429A/xx unknown
  • 1968-02-23 CH CH265968A patent/CH482716A/fr not_active IP Right Cessation
  • 1968-02-23 FI FI680478A patent/FI48275C/fi active
  • 1968-02-26 NO NO0696/68A patent/NO120734B/no unknown
  • 1968-02-28 SE SE02567/68A patent/SE337829B/xx unknown
  • 1968-02-28 DK DK78568AA patent/DK129198B/da not_active IP Right Cessation
  • 1968-02-29 ES ES351070A patent/ES351070A1/es not_active Expired
  • 1968-03-01 BE BE711546D patent/BE711546A/xx not_active IP Right Cessation
  • 1968-03-01 FR FR1562297D patent/FR1562297A/fr not_active Expired
  • 1968-03-01 YU YU0486/68A patent/YU31945B/xx unknown
  • 1968-05-28 FR FR153157A patent/FR7891M/fr not_active Expired

Patent Citations (1)

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